Home NDC 59137-570 Hexatrione
Product NDC 59137-570
11-digit product format 591370570
Labeler code 59137
Product ID 59137-570_5128fd5b-e866-907e-e063-6394a90ac4c9
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name triamcinolone hexacetonide
Dosage form INJECTION, SUSPENSION
Route INTRA-ARTICULAR
Labeler Medexus Pharma, Inc.
Marketing category UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Marketing start 2021-03-03
Substance TRIAMCINOLONE HEXACETONIDE
Active strength 40 mg/2mL
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Hexatrione
Brand name suffix 2%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRIAMCINOLONE HEXACETONIDE 40 mg/2mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination I7GT1U99Y9 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2539176 Internal RxNorm lookup 2539181 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59137-570-01 Hexatrione2% 2 mL in 1 AMPULE INJECTION, SUSPENSION 2 5 59137-570-01 Hexatrione2% 1 in 1 CARTON INJECTION, SUSPENSION 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59137-570 HEXATRIONE 2% (TRIAMCINOLONE HEXACETONIDE) INJECTION, SUSPENSION [MEDEXUS PHARMA, INC.] 3 Current NDC, Legacy NDC, 2 package rows 20230111_bc07ae9f-8a74-6bc8-e053-2995a90afc0d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59137-570-01 59137057001 1 AMPULE in 1 CARTON (59137-570-01) / 2 mL in 1 AMPULE 1 ampule 2026-05-05 2028-05-31 No No Current